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Catalog Number:
04027
CAS Number:
76757-90-9
Ester méthylique de boc-D-tyrosine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-Tyr-OMe
Documents
$18.53 /1G
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Informations sur le produit

Boc-D-tyrosine methyl ester is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Boc (tert-butyloxycarbonyl) group, which enhances its stability and solubility, making it an excellent choice for the synthesis of complex peptides. Researchers appreciate its role in facilitating the incorporation of D-tyrosine into peptide chains, which can be crucial for developing biologically active compounds and studying protein interactions. Its unique structure allows for selective reactions, providing chemists with the flexibility needed in various synthetic pathways.

In addition to its applications in peptide synthesis, Boc-D-tyrosine methyl ester is also valuable in the development of drug candidates, particularly in the fields of oncology and neurology, where modified amino acids can lead to improved therapeutic profiles. Its ability to enhance the bioavailability of certain compounds makes it a preferred choice among professionals seeking to optimize drug formulations. With its robust properties and practical applications, Boc-D-tyrosine methyl ester stands out as a key ingredient in modern chemical research and development.

Numéro CAS 
76757-90-9
Formule moléculaire
C 15 H 215
Poids moléculaire 
295.34
Rotation optique 
[a] D 20 = -49 ± 2º (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
76757-90-9
Formule moléculaire
C 15 H 215
Poids moléculaire 
295.34
Rotation optique 
[a] D 20 = -49 ± 2º (C = 1 dans CHCl 3 )
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Boc-D-tyrosine methyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly those that require protected amino acids. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, enhancing the efficiency of peptide formation.
  • Drug Development: In pharmaceutical research, it is used to create analogs of bioactive peptides, which can lead to the development of new therapeutic agents. Its ability to modify the structure of peptides can improve their efficacy and stability.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it can be linked to other molecules, such as drugs or imaging agents. This application is crucial in targeted drug delivery systems, enhancing the specificity of treatments.
  • Research in Neuroscience: Given its relation to tyrosine, it is used in studies exploring neurotransmitter pathways and their implications in neurological disorders, providing insights that could lead to novel treatments.
  • Cosmetic Formulations: Its derivatives are explored in cosmetic chemistry for their potential antioxidant properties, contributing to skin health and anti-aging products, appealing to the growing demand for effective skincare solutions.

Citations